The endogenous Mtv8 locus and the immunoglobulin repertoire

The vast diversity of mammalian adaptive antigen receptors allows for robust and efficient immune responses against a wide number of pathogens. The antigen receptor repertoire is built during the recombination of B and T cell receptor (BCR, TCR) loci and hypermutation of BCR loci. V(D)J recombinatio...

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Main Authors: Helen A. Beilinson, Steven A. Erickson, Tatyana Golovkina
Format: Article
Language:English
Published: Frontiers Media S.A. 2024-03-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2024.1345467/full
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author Helen A. Beilinson
Steven A. Erickson
Tatyana Golovkina
Tatyana Golovkina
Tatyana Golovkina
Tatyana Golovkina
author_facet Helen A. Beilinson
Steven A. Erickson
Tatyana Golovkina
Tatyana Golovkina
Tatyana Golovkina
Tatyana Golovkina
author_sort Helen A. Beilinson
collection DOAJ
description The vast diversity of mammalian adaptive antigen receptors allows for robust and efficient immune responses against a wide number of pathogens. The antigen receptor repertoire is built during the recombination of B and T cell receptor (BCR, TCR) loci and hypermutation of BCR loci. V(D)J recombination rearranges these antigen receptor loci, which are organized as an array of separate V, (D), and J gene segments. Transcription activation at the recombining locus leads to changes in the local three-dimensional architecture, which subsequently contributes to which gene segments are utilized for recombination. The endogenous retrovirus (ERV) mouse mammary tumor provirus 8 (Mtv8) resides on mouse chromosome 6 interposed within the large array of light chain kappa V gene segments. As ERVs contribute to changes in genomic architecture by driving high levels of transcription of neighboring genes, it was suggested that Mtv8 could influence the BCR repertoire. We generated Mtv8-deficient mice to determine if the ERV influences V(D)J recombination to test this possibility. We find that Mtv8 does not influence the BCR repertoire.
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spelling doaj.art-601882d9b48f4210b5bcabc749d861462024-03-05T04:59:40ZengFrontiers Media S.A.Frontiers in Immunology1664-32242024-03-011510.3389/fimmu.2024.13454671345467The endogenous Mtv8 locus and the immunoglobulin repertoireHelen A. Beilinson0Steven A. Erickson1Tatyana Golovkina2Tatyana Golovkina3Tatyana Golovkina4Tatyana Golovkina5Department of Microbiology, University of Chicago, Chicago, IL, United StatesDepartment of Immunobiology, Yale University, New Haven, CT, United StatesDepartment of Microbiology, University of Chicago, Chicago, IL, United StatesCommittee on Microbiology, University of Chicago, Chicago, IL, United StatesCommittee on Immunology, University of Chicago, Chicago, IL, United StatesCommittee on Genetics, Genomics and System Biology, University of Chicago, Chicago, IL, United StatesThe vast diversity of mammalian adaptive antigen receptors allows for robust and efficient immune responses against a wide number of pathogens. The antigen receptor repertoire is built during the recombination of B and T cell receptor (BCR, TCR) loci and hypermutation of BCR loci. V(D)J recombination rearranges these antigen receptor loci, which are organized as an array of separate V, (D), and J gene segments. Transcription activation at the recombining locus leads to changes in the local three-dimensional architecture, which subsequently contributes to which gene segments are utilized for recombination. The endogenous retrovirus (ERV) mouse mammary tumor provirus 8 (Mtv8) resides on mouse chromosome 6 interposed within the large array of light chain kappa V gene segments. As ERVs contribute to changes in genomic architecture by driving high levels of transcription of neighboring genes, it was suggested that Mtv8 could influence the BCR repertoire. We generated Mtv8-deficient mice to determine if the ERV influences V(D)J recombination to test this possibility. We find that Mtv8 does not influence the BCR repertoire.https://www.frontiersin.org/articles/10.3389/fimmu.2024.1345467/fullendogenous retrovirusimmunoglobulin repertoireV(D)J recombinationMTVB cell receptor (BCR) repertoire
spellingShingle Helen A. Beilinson
Steven A. Erickson
Tatyana Golovkina
Tatyana Golovkina
Tatyana Golovkina
Tatyana Golovkina
The endogenous Mtv8 locus and the immunoglobulin repertoire
Frontiers in Immunology
endogenous retrovirus
immunoglobulin repertoire
V(D)J recombination
MTV
B cell receptor (BCR) repertoire
title The endogenous Mtv8 locus and the immunoglobulin repertoire
title_full The endogenous Mtv8 locus and the immunoglobulin repertoire
title_fullStr The endogenous Mtv8 locus and the immunoglobulin repertoire
title_full_unstemmed The endogenous Mtv8 locus and the immunoglobulin repertoire
title_short The endogenous Mtv8 locus and the immunoglobulin repertoire
title_sort endogenous mtv8 locus and the immunoglobulin repertoire
topic endogenous retrovirus
immunoglobulin repertoire
V(D)J recombination
MTV
B cell receptor (BCR) repertoire
url https://www.frontiersin.org/articles/10.3389/fimmu.2024.1345467/full
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